Iodometric Redox Titration of Vitamin C Tablets

Iodometric Redox Titproportionn of Vitamin C get acrosstsIntroduction Vitamin C is a vital comp wholenessnt of a healthy diet which is why, desire many others, my father takes vitamin C supplements. However, I noniced that the vitamin C pills he takes expired in January 2009. These tablets were bought in the USA and breaked a lightsomeness amber tint. on that pointof, I wondered whether this would mean that over time, the density of vitamin C has decreased. Hence, I questi wizd a scientific system to determine the concent dimensionn of vitamin C in tell apart to see whether my father should continue using the expired tablets or rather buy new unitarys. Chemic tout ensembley cognize as ascorbic mordant, vitamin C is an organic compound containing of six carbon atoms, of which two muckle be readily oxidized under sedimentary caustic conditions or by air over a longer time period.The rule apply to mea trustworthy the concentration of vitamin C is c altogether tolded a reduction oxidisation, known as redox, titration. Ascorbic back breaker reacts with one (I2) to create dehydroascorbic savage (C6H8O6) under stingingic sedimentary conditionsC6H8O6 (aq) + I2 (aq) C6H6O6 (aq) + 2 I(aq) + 2 H+(aq) However, as iodine I2 is non actu aloney dissolvable in irrigate supply, a complex created by sedimentary iodine I2 (aq) and aqueous iodide anion I(aq) through the following chemical reaction essential be wont.I2 (aq) + I(aq) I3(aq) I3 is known as triiodide, which is much more soluble in water than iodine. The method utilize to create the triiodide is the reaction of aqueous io fancy IO3(aq) with aqueous iodide I(aq) under acidic aqueous conditions as shown below.Reaction 1IO3(aq) + 8 I(aq) + 6 H+(aq) 3 I3(aq) + 3 H2O (l) The reaction of water soluble amylum, being a white solving, with triiodide gives a unconsolable blue complex. This alteration of coloration shows the give up of the redox titration.The redox titration is using t he reaction of aqueous triiodide I3 (aq) with aqueous ascorbic acid C6H8O6 (aq) to piddle aqueous dehydroascorbic acid C6H6O6 (aq) and aqueous iodide I(aq) under acidic aqueous conditions.Reaction 2 C6H8O6 (aq) + I3 (aq) C6H6O6 (aq) + 3 I(aq) + 2 H+(aq) The method use is an corroborative titration, which means it measures the arrive of triiodide remain in the beginning after having reacted with the ascorbic acid. Therefore an excess of aqueous triiodide I3 (aq) is needed.The excess aqueous triiodide I3 (aq) is reduced by aqueous thiosulfate S2O32- (aq) to create aqueous iodide I(aq) and aqueous tetrathionate S4O62- (aq) as shown below.Reaction 3I3 (aq) + 2 S2O32- (aq) 3 I (aq) + S4O62- (aq) As soon as all the triiodide is reduced to iodide, the colour changes from dark blue (the triiodide amylum complex is dark blue) to white. The oxidisation of ascorbic acid is a 11 reaction, meaning 1 counterspy of ascorbic acid regards 1 seawalle of triiodide to form 1 jetty of dehydroascorbic acid, whereas the oxidation of thiosulfate is a 12 reaction, meaning 2 bulwark of thiosulfate can be oxidized to 1 mol tetrathionate by 1 mol of triiodide, all under acidic conditions in water. Knowing this one can envision the amount of vitamin C in various tablets as long as all of them be readily soluble in water, meaning, for example, not coated.(CH 212 denary Analysis. 1-2)Research QuestionWhat is the effect of the age of vitamin C tablets, expressed by the scrap of months elapsed after the expiry date, on the concentration in destiny tilt of vitamin C in said tablets?VariablesVariableUnit consecrateMethod of measurementIn bloodsuckingNumber of months after expiry date of vitamin CDate withmonth, year01/2009 = 92 months 09/2014 = 24 months 07/2015 = 14 months 04/2018 = 0 monthsThe expiration date of the vitamin C tablet / sachet is written on the out well-nigh promotional materialDependent Concentration of vitamin C% weight0 atomic itemise 6%Content of vitamin C in mg per tablet is written on the outer packaging and measured through titrationControlled VariablesUnitPossible effect(s) on resultsMethod for controlNumber of tablets / sachetsn/a violate weight of vitamin CCounting tablets / sachetsConcentration of atomic function 11 thiosulfate (Na2S2O3 (aq)) cat valium iodate (KIO3 (aq))mol/lmol/l impose on _or_ oppress concentration of vitamin CTitration with (KIO3 (aq))Analytical shieldConcentration of Starch Sodium carbonate Sulphuric acidg/lg/lmol/lNo significant impact on dependent variableAnalytical pieceed seriesAnalytical cuticle50 ml criterion cylinderConcentration of Potassium iodide (KI (aq))mol/lWrong concentration of triiodide solutionAnalytical scaleMaterials1 g of soluble amylum8 M (mol/l) sulfuric acid (H2SO4) purePotassium iodide (KI), 95%, pure, DABPotassium iodate (KIO3), p. A. EMSURE ACS, ISO, Ph Eurpure, DABVitamin C (ascorbic acid (C6H8O6))tablets or sachets (it is recommended to use colour little dissolvable products, otherwise the colour change will be difficult to see)Sodium thiosulfate pentahydrate (Na2S2O3 5H2O), 99,5%, pure, DABSodium carbonate (Na2CO3) 99,5%, pure, DABDistilled water (H2O)ApparatusOne 3 ml 0,01 ml amount pipetteTwo 250 ml 5% beakers and two calciferol ml 5% beakersOne 50 ml 0,08 ml and one 100 ml 0,1 ml measuring cylinderTwo euchre ml 0,2 ml quite a littletric flaskfuls with a corkThree 250 ml Erlenmeyer flasks to be used for the titrationsOne 50 ml 0,1 ml buret with stand and secure for buretteTwo funnels, distributively with a diameter of 9,5 cmIt is necessary to fresh and rinse all glassware with distilled water out fronthand to avoid impurities and contamination of solution used.One electric scale set in grams and preferably to four decimal places g 0,1 mg to allow for maximum accuracy (available scale had two decimal places g 10 mg)One magnetic stirrer, one aspiration rod and a daub with a pestleSmall spoons, scalpels and cups , in total 5 of all(prenominal)Rubber gloves and safety glasses as the reactants used can irritate skin and eyesMethod Preparation of starch index numberFill a 250 ml beaker with 100 ml of distilled water, measured with a 50 ml cylinder.Weigh 1 g of soluble starch using the scale and a spoon. Add the starch to the beaker. victimization the stirring rod, stir until dissolved. Every day a new solution should be made.Preparation of sodium thiosulfateUse a 100 ml measuring cylinder to fill 450 ml of distilled water into a euchre ml beaker.Weigh 0,05 g of Na2CO3 using the scale, a spoon, and a cup and come to beaker.Weigh 8,7 g of Na2S2O3 5H2O using the scale, a spoon, and a separate, equally pretty small cup. Add to the same beaker.Dissolve the chemicals compounds through swirling the beaker.Once dissolved, displace the solution into a idle vitamin D ml volumetric flask and render distilled water up to exactly 500 ml. Seal it tightly with the cork. evaluate the solution as so dium thiosulfate. Keep the flask disagreeable when not in use.Preparation of standard iodate solutionUse a 100 ml measuring cylinder to fill 450 ml of distilled water into a 500 ml beaker.Weigh 1,01 g of KIO3 in a small, clean cup using the scale and a clean spoon. rain buckets the KIO3 into the 450 ml of distilled water. fiddle with the beaker until the potassium iodate has completely dissolved.Once dissolved, pour the solution into a clean 500 ml volumetric flask and add distilled water up to exactly 500 ml. Seal it tightly with the cork. Label the solution as potassium iodate. Keep the flask closed when not in use. warningising the sodium thiosulfate solution order up the stand and clamp for the 50 ml burette.Fill the closed 50 ml burette with the previously disposed(p) sodium thiosulfate solution using a clean funnel. It is vital that the burette contains precisely 50 ml.Using a 50 ml measuring cylinder pour exactly 50 ml of the KIO3 solution into a clean 250 ml Erlenmeyer fla sk.Weigh 2 g of KI in a small cup using the scale and a spoon. come to the fore the KI into the flask.Add 5 ml of 8 M H2SO4 into the flask using a 50 ml measuring cylinder.Place the 250 ml Erlenmeyer flask onto a magnetic stirrer and get down stirring it. This is to ensure that all the reactants in the solution take a leak reacted to form the triiodide molecule.The solution should have a dark red colour collectable to the presence of triiodide. Titrate the solution with sodium thiosulfate until the solution has lost most of its red, i.e. a light shade of scandalmongering appears. Using the 3 ml measuring pipette, add 2 ml of the starch indicator to the solution. The starch is whole added shortly before the end point of the titration as front to this, the triiodide starch complex locks onto the triiodide and thus the triiodide might not react with the sodium thiosulfate. carry titrating the solution until the solution has become colourless. Record the amount of ml of sodium th iosulfate solution used.Repeat the titration three times in order to obtain reliable values, as this titration tells us the exact concentration of sodium thiosulfate, which allows us to determine the amount of triiodide.Titration of ascorbic acidUse a 50 ml measuring cylinder to fill 15 ml of 8 M H2SO4 into a clean 250 ml Erlenmeyer flask used for titration. Using a 100 ml measuring cylinder add 75 ml of distilled water.Grind vitamin C tablets separately and thoroughly with a mortar and pestle. Put them into the flask and stir until fully dissolved. If needed, for example if part of the tablet is not soluble any longer, filter the solution by using a funnel and filter paper.Carefully pour the solution into a clean 250 ml Erlenmeyer flask used for titration.Using a 50 ml measuring cylinder pour 50 ml of KIO3 solution into the 250 ml Erlenmeyer flask used for the titration.Weigh 2 g of KI in a small cup using the scale and a spoon. Place the KI into the 250 ml Erlenmeyer flask used fo r the titration. At this point, the solution should develop a dark shade of red due to the presence of triiodide.Swirl the flask to make sure the reaction between triiodide and ascorbic acid has been completed.Set up the stand and clamp for the 50 ml burette.Place the 250 ml Erlenmeyer flask used for the titration onto a magnetic stirrer, and begin stirring it. This ensures that the vitamin C has truly completely reacted.Fill the closed 50 ml burette with sodium thiosulfate solution using a clean funnel. Ensure that the burette was cleaned beforehand and remove any excess solution.Begin titrating the triiodide solution with sodium thiosulfate. It should start out being red due to the presence of adit triiodide. When the solution changes to a pale yellow, add 2 ml of the starch indicator using a 3 ml measuring pipette. same to the previous titration, the starch might hold onto the triiodide and prevent it from reacting with sodium thiosulfate. Continue titrating the solution until it has become colourless. Due to various colourings of the tablets, this might be an off-shade of white. name this volume as the end point of the titration.Repeat steps 21-31 for all tablets and sachets available. Each specimen of tablets or sachets should be titrated at least tailfin times in order to calculate a representative amount of vitamin C contained in the tablets. It is important to note that the flask containing the vitamin C solution and the magnet of the magnetic stirrer must be washed before each trial to avoid impurities. (CH 212 Quantitative Analysis. 5-7)Safety ConsiderationsMake sure that safety glasses and gloves are used during the experiment. Appropriate safety garb must be worn, like laboratory coats with long sleeves. Content of solutions prepared need to be clearly marked with water proof pencils and locked apart in laboratory cupboards. Any solution not used anymore needs to be placed it appropriate waste disposal units. fling off any acids before dis posing of them. Raw Data submit 1 shows the overview of all the samples used in the iodometric redox titrations. renderReferenceNumberExpiry dateMonths till Sep. 2016Number of tablets/ sachets usedWeight of tablet/sachet gstated by manufacturerVitamin C in mg per tablet/sachet stated by manufacturerVitamin C USP tablet1Jan. 20099211No value given500Heie Zitrone sachet2Sep. 201424110180Vitamin C Arancia tablet3Jul. 20151424 = 84,590Vitamin CZitrone tablet4Apr. 20180104180Table 1 Samples used in the titrationTable 2 shows the volume of sodium thiosulfate involve to titrate 50 ml of potassium iodate.Titration 1Titration 2Titration 3Volume in ml of sodium thiosulfate solution39,0 0,138,6 0,138,6 0,1Table 2 Volume of sodium thiosulfate solutionNote As the fate perplexity of titration 1 0,25% and titration 1 and 2 is 0,26%, these uncertainty are not interpreted into account, as there is very little impact on the results. Table 3 shows the results of all titrations of the vitamin C s amples.Sample NumberVolume in ml of sodium thiosulfate solution required to titrate rest triiodide ( 0,1)1 504,63,13,93,63,73,43,43,33,63,8217,4316,519,215,314,2413,414,31313,812,415,314,410,612,511,2Table 3 Volume of sodium thiosulfate solution in ml used in the titrationsIt was observed that the colour changed from dark blue to a pale yellow as the sample was titrated due to the reaction of triiodide with thiosulfate.Calculations and Processed ResultsIn order to find the percentage of vitamin C in each sample, one must calculate the exact concentration of sodium thiosulfate used in all titrations.8,7 g Na2S2O3 5H2O with molar mass 248,2 g/mol in 500 ml water = 0,070109 mol/l S2O32 molar(a) ratio of the oxidation of S2O32- is S2O32-I3 = 2138,73 ml of 0,070109 mol/l S2O32- = 0,002715 mol S2O32- are oxidized by 0,001358 mol I3wedge ratio of the creation of I3 is IO3 I3 = 130,001358 mol I3 = 0,000453 mol IO3 in 50 ml = 0,009051 mol/l IO3Exact concentration of KIO3 = 1,01 g KIO3/500 ml = 0,009439 mol/l IO3 Exact concentration of S2O32- is higher by a portion of 0,009439/0,009051 = 1,042911 Exact concentration = 0,070109 1,042911 = 0,073117 mol/l S2O32-Table 4 shows the volume and concentration of sodium thiosulfate used.Titration Numberml Na2S2O3used ( 0,1)ml Na2S2O3arithmetic intermediate hypothetic concentration Na2S2O3 mol/lExperimental/Exact concentrationNa2S2O3 mol/l139,0038,73 0,3238,600,0701090,073117338,60Table 4 Calculation of concentration of sodium thiosulfateNote As the uncertainty of 38,73 ml 0,3 gives a percentage uncertainty of 0,77%, this uncertainty are not taken into account, as there is very little impact on the results. In knowing two the precise concentration of sodium thiosulfate and the volume needed to titrate the remaining triiodide, one can determine the concentration of vitamin C in each sample as there is an excess of KIO3 present in each titration.Reaction 2 C6H8O6 (aq) + I3 (aq) C6H6O6 (aq) + 3 I(aq) + 2 H+(aq)Molar ratio of I3C6H8O6 = 11 Molar ratio of IO3I3 = 13 Molar ratio of IO3C6H8O6 = 13 50 ml 0,009439 mol/l KIO3 = 0,000472 mol IO3 = 3 times more moles of vitamin C 0,000472 3 = 0,001416 mol vitamin C = 249,4 mg vitamin COnly the offset sample had a theoretical maximum content of 500 mg, which is more than the 50 ml of 0,009439 mol/l IO3 solution can oxidize, that means no triiodide should have been left over and therefore the blue starch triiodide complex should not have been formed. However, in each titration a blue colour was visible. Therefore, the method utilize was valid for all other titrations, otherwise the weight of the sample should have been reduced.Reaction 3I3 (aq) + 2 S2O32- (aq) 3 I (aq) + S4O62- (aq)Molar ratio of I3 S2O32- = 12The arithmetic average of 10 titrations of the branch sample is 3,64 ml of 0,073117 mol/l S2O32- used to titrate the remaining I3. 3,64 ml of 0,073117 mol/l S2O32- = 0,000266 mol S2O32- are oxidized by 0,000133 mol I3. After the reaction of 50 ml of 0,009439 mol/l IO3 solution with the vitamin C sample 0,000133 mol I3 were left over.Molar ratio of IO3I3 = 1350 ml 0,009439 mol/l IO3= 0,000472 mol IO3 = 0,001416 mol I3 0,001416 mol I3 at the start of the reaction 0,000133 mol I3 found after the reaction = 0,001283 mol reacted with vitamin CMolar ratio of I3C6H8O6 = 110,001283 mol I3 = 0,001283 mol C6H8O6 = 0,001283 mol 176,1 g/mol = 225,9 mg vitamin C 500 mg vitamin C = 100% and 225,9 mg vitamin C = 45,19% active content.This method is applied to all results. Table 5 shows the results of titrating the four different vitamin C samples.Sample0,073117 mol/l Na2S2O3 solution in ml usedTablets/ SachetVitamin C (mg)Vitamin CAgeNo.Arithmetic average/Number of titrationsStandard deviationNo. used in titrationWritten on packagingFound via titration% found via titrationMonths expired1 3,64 / 100,41150022645,1992217,40 / 1118013776,3024316,30 / 42,152 9014480,2414413,09 / 101,39118016591,720Table 5 reason and measured results of titrati on of Vitamin C samplesMonths expired is the time elapsed between the expiry date and the month of the laboratory work in September 2016. The first titration of sample 1 (see table 3) was an outlier and not considered when calculating the arithmetic average and standard deviation. Only one sachet of sample 2 was available, thus not allowing to calculate average and standard deviation. Graph 1 shows the percentage of Vitamin C found and the age of the tablets and sachet used.Graph 1Correlation of concentration of Vitamin C versus number of months expired Graph 2 shows that the reliabilty of the result depends on the number of titrations carried out. The var. of the results is two times standard deviation ( 2 ).Graph 2 Concentration of vitamin C and error bar of 2 (sample 2 was only titrated once, thus no standard deviation can be calculated) assumptive that the results are following a normal distribution, 95,4% of the titrations are within the 2 range as shown above. Thus, the r esults are accepted for sample 1, 3 and 4. consequence and EvaluationThe results show that the vitamin C content decreases over time. This is demonstrated in graph 1, as the slope is -0,048. The coefficient of determination is 0,989, which is close to 1 and therefore shows a strong linear correlation. This means the results clearly demonstrate that as the number of months expired increases, the concentration of vitamin C decreases. These findings are supported by research of the Applied Sciences Department at the Osun State Polytechnic in Iree, Nigeria, make in 2012. (Oyetade 22) High temperature, exposure to air and sunlight accelerate the oxidation of vitamin C. Thus, the oldest sample shows the highest reduction in percentage concentration of vitamin C with 45,19%, less than half. This means that my father should buy new vitamin supplements, and no longer use his old ones, which were sample 1. Strengths The method of investigation delivers fast results, does not require expensi ve equipment, and works with chemicals that are neither very toxic nor highly harmful to the environment. A clear relationship between the variables was demonstrated and due to relatively low standard deviation, the results are accepted. Weaknesses Potential errors were detected. Only one sachet of sample 2 was available, thus not meeting the minimum criteria of at least 3 titrations of each sample. It is also possible that not all the triiodide reacted with the sodium thiosulfate (see step 18 in methodology). In terms of method, the equipment used was not precise enough, causing possible systematic errors. Instead of a measuring cylinder a volumetric pipette should have been used as well as a high precision scale 0,1 mg. Not all samples were easily soluble in water and produced a clear and colourless solution, thus the end of titration was difficult to notice, leading to inaccuracies. The thiosulfate and iodate solutions should not have been stored over a long time exposed to unr estrained temperature and day light. All titrations should either have been done in one day or the titrants should have been stored in a cool and dark place.Works CitedCH 212 Quantitative Analysis. Philadelphia La Salle University, n.d. PDFOyetade, O. A., G. O. Oyeleke, B. M. Adegoke, and A. O. Akintunde. Stability Studies on Ascorbic Acid (Vitamin C) From divers(prenominal) Sources. N.p. IOSR Journal of Applied Chemistry (IOSR-JAC), Sept.-Oct. 2012. PDF.